Canonical Allele Identifier: CA2692654819

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136676919-G-GCCCCCCCCCCAACCCCCCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676919_136676920insCCCCCCCCCCAACCCCCCCA , CM000671.2:g.136676919_136676920insCCCCCCCCCCAACCCCCCCA	GRCh38
NC_000009.11:g.139571371_139571372insCCCCCCCCCCAACCCCCCCA , CM000671.1:g.139571371_139571372insCCCCCCCCCCAACCCCCCCA	GRCh37
NC_000009.10:g.138691192_138691193insCCCCCCCCCCAACCCCCCCA	NCBI36
NG_008090.1:g.15540_15541insTGGGGGGGTTGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+41_492+42insTGGGGGGGTTGGGGGGGGGG MANE Select	ENSP00000360761.2:n.492+41_492+42insTGGGGGGGTTGGGGGGGGGG
ENST00000371694.7:c.492+41_492+42insTGGGGGGGTTGGGGGGGGGG	ENSP00000360759.3:n.492+41_492+42insTGGGGGGGTTGGGGGGGGGG
ENST00000371696.6:c.492+41_492+42insTGGGGGGGTTGGGGGGGGGG	ENSP00000360761.2:n.492+41_492+42insTGGGGGGGTTGGGGGGGGGG
ENST00000472820.1:n.420+41_420+42insTGGGGGGGTTGGGGGGGGGG
ENST00000538402.1:c.492+41_492+42insTGGGGGGGTTGGGGGGGGGG	ENSP00000438919.1:n.492+41_492+42insTGGGGGGGTTGGGGGGGGGG
NM_001012727.1:c.492+41_492+42insTGGGGGGGTTGGGGGGGGGG	NP_001012745.1:n.492+41_492+42insTGGGGGGGTTGGGGGGGGGG
NM_006412.3:c.492+41_492+42insTGGGGGGGTTGGGGGGGGGG	NP_006403.2:n.492+41_492+42insTGGGGGGGTTGGGGGGGGGG
NM_006412.4:c.492+41_492+42insTGGGGGGGTTGGGGGGGGGG MANE Select	NP_006403.2:n.492+41_492+42insTGGGGGGGTTGGGGGGGGGG
NM_001012727.2:c.492+41_492+42insTGGGGGGGTTGGGGGGGGGG	NP_001012745.1:n.492+41_492+42insTGGGGGGGTTGGGGGGGGGG